Modified geopolymer compositions, processes and uses

ABSTRACT

The present invention relates to modified geopolymer compositions, geopolymer-coated organic polymer substrates, and methods of manufacturing and articles comprising same.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims benefit from U.S. Provisional Patent ApplicationNo. 61/181,870, filed May 28, 2009, the entire contents of which arehereby incorporated herein by reference.

STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT

Not applicable.

THE NAMES OF PARTIES TO A JOINT RESEARCH AGREEMENT

Not applicable.

INCORPORATION-BY-REFERENCE OF MATERIAL SUBMITTED ON A COMPACT DISC

Not applicable.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to modified geopolymer compositions,geopolymer-coated organic polymer substrates, and methods ofmanufacturing and articles comprising same.

2. Description of Related Art

Geopolymer materials have been used in construction (e.g., to makebricks) for centuries. Geopolymer compositions contain elements thatinclude hydrogen, aluminum, silicon, oxygen, and a metal of Group 1 ofthe Periodic Table of the Elements.

Recently, Belaguru mentions, among other things, geopolymer compositionsuseful for coating surfaces of concrete, steel, or wood (Belaguru P.,Geopolymer for Protective Coating of Transportation Infrastructures,FINAL REPORT, Report Number FHWA NJ 1998-12, 1998, Rutgers, The StateUniversity, Piscataway, N.J.). There Belaguru also mentions somecompositions that comprise or are prepared with, among other things, anunspecified polymer latex. The exemplified polymer latex-containingcompositions of Belaguru (see Composition 1 and Sample ID 28 to 36 inTable 1) comprise, among other things, “potassium silicate” (K₂SiO₃), a“silica fume” (“SiO₂”), and “ground sand,” but do not seem to contain aningredient that functions as a significant source of aluminum (e.g., asin aluminum oxides characteristic of geopolymer). Thus, the polymerlatex-containing compositions of Belaguru do not seem to comprisegeopolymer.

WO 2008/017413 A1 mentions pumpable geopolymer formulation andapplication for carbon dioxide storage.

There is a need in the art for modified geopolymer compositions usefulfor coating organic polymer substrates, geopolymer-coated organicpolymer substrates, and methods of manufacturing the same.

BRIEF SUMMARY OF THE INVENTION

In a first embodiment, the present invention provides a modifiedgeopolymer composition that comprises either (i) a stabilizedgeopolymer-organic polymer latex composition comprising a mixture of ageopolymer and an organic polymer latex; or (ii) a highly organicpolymer-adherent capable, modified geopolymer composition. In someembodiments the modified geopolymer composition comprises the stabilizedgeopolymer-organic polymer latex composition, preferably wherein themixture is essentially uniform. In some embodiments the stabilizedgeopolymer-organic polymer latex composition comprises the highlyorganic polymer-adherent capable, modified geopolymer composition. Insome embodiments, the modified geopolymer composition does not contain acalcium based oxide. As used herein, the term “highly organicpolymer-adherent capable” means characterizable as being able, afterbeing cured and dried, to bond to a coating-ready surface of an organicpolymer substrate (e.g., a surface of an extruded polystyrene foamsubstrate) with a bond strength of 50 kilopascals (kPa) or greater. Apreferred method for measuring the bond strength is a tensile pull testmethod, which is described later. In some embodiments the stabilizedgeopolymer-organic polymer latex composition comprises, or is formed bycombining, a first mixture of a hydrated polysialate and from 1.0 weightpercent to 50 weight percent of an organic polymer latex; weight percentof the organic polymer latex being based on total weight of the firstmixture. In some embodiments, the organic polymer latex, which is usedto form the first mixture, comprises an organic polymer latex powder(i.e., the organic polymer latex powder is not water borne). In otherembodiments, the organic polymer latex, which is used to form the firstmixture, comprises a second mixture that comprises a water-borne organicpolymer latex and from 0.05 weight percent to 10 weight percent of alatex stabilizer, weight percent of the latex stabilizer being based ontotal weight of the second mixture

Preferably, the highly organic polymer-adherent capable, modifiedgeopolymer composition is a water concentration- and silicon/aluminum(Si/Al) molar ratio-modified geopolymer composition, the waterconcentration- and Si/Al molar ratio-modified geopolymer compositionhaving less than 36.0 weight percent of water based on total weight ofthe water concentration- and Si/Al molar ratio-modified geopolymer and aSi/Al molar ratio of greater than or equal to 1.70. More preferably, theSi/Al molar ratio is greater than or equal to 1.70 and less than orequal to 3.0.

In a second embodiment, the present invention provides a method ofpreparing a geopolymer-coated organic polymer substrate comprising adried modified geopolymer layer in adhering operative contact with anorganic polymer substrate, the adhering operative contact beingcharacterizable as having a bond strength of 25 kilopascals (kPa) orgreater as measured according to the tensile pull test method, themethod comprising forming the geopolymer-coated organic polymersubstrate as a function of drying a modified geopolymer precursor layer,the modified geopolymer precursor layer being in contact with theorganic polymer substrate.

In some embodiments, the method of the second embodiment furthercomprises a preliminary step of curing the precursor modified geopolymerlayer to give a cured modified geopolymer precursor layer. Morepreferably, the curing step is essentially simultaneous with, or stillmore preferably, at least partially precedes (i.e., some curing occursbefore drying) or substantially precedes (most or all curing occursbefore drying), the drying step. In some embodiments the curingsubstantially precedes the drying. In some embodiments, the modifiedgeopolymer precursor layer comprises the cured modified geopolymerprecursor layer. Still more preferably, the method of the secondembodiment comprises steps of: (a) providing the organic polymersubstrate, the organic polymer substrate having a coating-ready surface;(b) contacting one of the modified geopolymer compositions of the firstembodiment to the coating-ready surface, or a portion thereof, of theorganic polymer substrate to give the modified geopolymer precursorlayer in physical contact with the coating-ready surface, or the portionthereof, of the organic polymer substrate; (c) curing the modifiedgeopolymer precursor layer to give the cured modified geopolymerprecursor layer; and (d) drying the cured modified geopolymer precursorlayer so as to remove at least 25 weight percent of water therefrom togive the geopolymer-coated organic polymer substrate.

In the second embodiment, the (cured) modified geopolymer precursorlayers independently are in physical contact with the coating-readysurface, or the portion thereof, of the organic polymer substrate. Insome embodiments, the cured and dried modified geopolymer layer, curedmodified geopolymer precursor layer, and modified geopolymer precursorlayer respectively comprise a cured and dried, highly organicpolymer-adherent capable, modified geopolymer composition layer; a curedhighly organic polymer-adherent capable, modified geopolymer compositionprecursor layer; and a highly organic polymer-adherent capable, modifiedgeopolymer composition precursor layer. The highly organicpolymer-adherent capable, modified geopolymer composition precursorlayer is formed from the highly organic polymer-adherent capable,modified geopolymer composition of the first embodiment.

In some embodiments, the cured and dried modified geopolymer layer,cured modified geopolymer precursor layer, and modified geopolymerprecursor layer respectively comprise a cured and dried,geopolymer-organic polymer latex layer; a cured geopolymer-organicpolymer latex precursor layer; and a geopolymer-organic polymer latexprecursor layer. The geopolymer-organic polymer latex precursor layer isformed from the stabilized geopolymer-organic polymer latex compositionof the first embodiment. In embodiments of the method of the secondembodiment that employ the cured geopolymer-organic polymer latexprecursor layer, the organic polymer latex is characterizable as havinga glass transition temperature and the drying step is characterizable ashaving a drying temperature, the drying temperature of the drying stepbeing greater than the glass transition temperature of the organicpolymer latex.

In a third embodiment, the present invention provides ageopolymer-coated organic polymer substrate comprising a dried modifiedgeopolymer layer in adhering operative contact with a coating-readysurface, or portion thereof, of an organic polymer substrate, theadhering operative contact being characterizable as having a bondstrength of 25 kilopascals (kPa) or greater as measured according to thetensile pull test method. Preferably the geopolymer-coated organicpolymer substrate is prepared by the method of the second embodiment.

The invention geopolymer-coated organic polymer substrates are useful,for example, in applications and articles where it is desirable for thegeopolymer-coated organic polymer substrate to have an enhancedaesthetic appearance or, preferably, improved flame-, heat-, light-,mechanical-, or chemical-resistance property, or a combination of two ormore properties thereof, compared to such respective aestheticappearance, property or properties of the uncoated organic polymersubstrate. The dried modified geopolymer layer, including such layerprepared by the method of the second embodiment, provides saidresistance properties to the organic polymer substrate to which it isadhered or bonded in the geopolymer-coated organic polymer substrate.Thus the invention geopolymer-coated organic polymer substrates areuseful for preparing articles such as, for example, automotivecomponents such as, for example, automotive hoses; building componentssuch as, for example, external and internal building cladding (e.g., anexterior insulation and finishing system); outdoor articles such as, forexample, outdoor furniture and signage; and lined infrastructurecomponents such as, for example, lined industrial piping (e.g., linedsewer, water, and chemical process piping). The geopolymer articles alsocomprise housings such as, for example, electronic device and batteryhousings.

The invention modified geopolymer composition is capable of coating acoating-ready surface of an organic polymer substrate and, after curingand drying (e.g., hardening and removing a substantial amount of thewater from the modified geopolymer composition), forming an adherent,preferably highly adherent, coating layer on the coating ready surfaceof the organic polymer substrate. In contrast to the invention modifiedgeopolymer compositions, non-invention compositions consisting ofunmodified geopolymer or non-invention modified geopolymer, after curingand drying, do not adhere, or adhere weakly (e.g., with a bond strengthof less than 22 kPa, in some cases less than 11 kPa, when measured bythe tensile pull test method described later) to coating-ready surfacesof organic polymer substrates.

Additional embodiments are described in the remainder of thespecification, including the claims.

DETAILED DESCRIPTION OF THE INVENTION

The embodiments of the present invention described previously areincorporated by reference here. Those embodiments and the additionalembodiments described later are further illustrated with reference tothe following information.

For purposes of United States patent practice and other patent practicesallowing incorporation of subject matter by reference, the entirecontents—unless otherwise indicated—of each U.S. patent, U.S. patentapplication, U.S. patent application publication, PCT internationalpatent application and WO publication equivalent thereof, referenced inthe instant Detailed Description of the Invention are herebyincorporated by reference. In an event where there is a conflict betweenwhat is written in the present specification and what is written in apatent, patent application, or patent application publication, or aportion thereof that is incorporated by reference, what is written inthe present specification controls.

In the present application, any lower limit of a range of numbers, orany preferred lower limit of the range, may be combined with any upperlimit of the range, or any preferred upper limit of the range, to definea preferred aspect or embodiment of the range. Each range of numbersincludes all numbers, both rational and irrational numbers, subsumedwithin that range (e.g., the range from about 1 to about 5 includes, forexample, 1, 1.5, 2, 2.75, 3, 3.80, 4, and 5).

In an event where there is a conflict between a compound name and itsstructure, the structure controls.

In an event where there is a conflict between a unit value that isrecited without parentheses, e.g., 2 inches, and a corresponding unitvalue that is parenthetically recited, e.g., (5 centimeters), the unitvalue recited without parentheses controls.

As used herein, “a,” “an,” “the,” “at least one,” and “one or more” areused interchangeably. In any aspect or embodiment of the instantinvention described herein, the term “about” in a phrase referring to anumerical value may be deleted from the phrase to give another aspect orembodiment of the instant invention. In the former aspects orembodiments employing the term “about,” preferably it means from 90percent to 100 percent of the numerical value, from 100 percent to 110percent of the numerical value, or from 90 percent to 110 percent of thenumerical value. In any aspect or embodiment of the instant inventiondescribed herein, the open-ended terms “comprising,” “comprises,” andthe like (which are synonymous with “including,” “having,” and“characterized by”) may be replaced by the respective partially closedphrases “consisting essentially of,” consists essentially of,” and thelike or the respective closed phrases “consisting of,” “consists of,”and the like to give another aspect or embodiment of the instantinvention. In the present application, when referring to a precedinglist of elements (e.g., ingredients), the phrases “mixture thereof,”“combination thereof,” and the like mean any two or more, including all,of the listed elements. The term “or” used in a listing of members,unless stated otherwise, refers to the listed members individually aswell as in any combination, and supports additional embodiments recitingany one of the individual members (e.g., in an embodiment reciting thephrase “10 percent or more,” the “or” supports another embodimentreciting “10 percent” and still another embodiment reciting “more than10 percent.”). The term “plurality” means two or more, each pluralitybeing independently selected unless indicated otherwise. As used herein,“weight percent” and “wt %” are synonymous and are calculated for acomponent of a mixture based on total weight of the mixture unlessindicated otherwise.

The term “layer” means a coating or film of a material. The term“coating-ready surface” means an area exposed to and prepared to receivea material for coating thereof.

The “glass transition temperature” (T_(g)) is determined by differentialscanning calorimetry using a differential scanning calorimeter accordingto the method of ASTM E1356-03.

A mixture “comprising, or formed by combining” means a blend of or amaterial derived (e.g., chemically) from, or both.

Unless otherwise noted, the phrase “Periodic Table of the Elements”refers to the official periodic table, version dated Jun. 22, 2007,published by the International Union of Pure and Applied Chemistry(IUPAC). Also any references to a Group or Groups shall be to the Groupor Groups reflected in this Periodic Table of the Elements.

The term “geopolymer” means a three-dimensional inorganicaluminosilicates mineral polymer that comprises a hydrated polysialate.Preferably, the hydrated polysialate is of empirical formula (G):(M)_(y)[-(-SiO₂)_(z)—AlO₂)]_(x) .wH₂O  (G),wherein each M independently is a cation of Group 1 of the PeriodicTable of the Elements; x is an integer of 2 or higher and represents anumber of polysialate repeat units; y is an integer selected so that aratio of y to x is greater than zero (y/x>0), preferably from greaterthan zero to less than or equal to 1 (0<y/x<1); z is a rational orirrational number of from 1 to 35; and w is a rational or irrationalnumber such that ratio of w to x (w/x) represents a ratio of moles ofwater per polysialate repeat unit. The z represents a molar ratio equalto moles of silicon atoms to moles of aluminum atoms (Si/Al) in thepolysialate. The distribution of the SiO₂ functional groups in theinvention geopolymer composition may be characterizable as being random.Thus, z can be a rational or irrational number.

In the hydrated polysialate of empirical formula (G), the w ispreferably chosen to give a “geopolymer viscosity effective amount” ofwater, which means a quantity of water sufficient to a establish adesired resistance to flow for the stabilized geopolymer-organic polymerlatex composition of the first embodiment such that the method of thesecond embodiment can be accomplished. More preferably, w is a rationalor irrational number of from about 4 to about 8, more preferably from 4to about 7.5. To give a desired geopolymer viscosity effective amount ofwater in the stabilized geopolymer-organic polymer latex composition,the w can be adjusted higher or lower by adding water to or removing(such as by drying) some water from the stabilized geopolymer-organicpolymer latex composition.

In the hydrated polysialate of empirical formula (G), preferably each Mindependently is a cation of one or more metals of Group 1 of thePeriodic Table of the Elements. Most common cations comprise potassiumcation (K⁺), sodium cation (Na⁺), lithium cation (Li⁺), or a combinationof two or more thereof. In some embodiments, the cations may furthercomprise cations of one or more metals of Group 2 of the Periodic Tableof the Elements, more preferably magnesium cation (Mg⁺²), and still morepreferably calcium cation (Ca⁺²). In such embodiments, preferably thecalcium cation does not comprise, and is not derived from, a calciumoxide. Preferably, at least 51 mol %, more preferably at least 90 mol %,still more preferably at least 98 mol %, and even more preferably atleast 99 mol % of M are Na⁺.

In the hydrated polysialate of empirical formula (G), preferably z is arational or irrational number of from 1 to 3. In some embodiments, z isbetween 2 and 3 or, preferably, between 1 and 2. Preferably, z is 1.70or greater and, more preferably, 1.9 or greater. Preferably, z is 3.0 orless. In some embodiments, z is 2.0 or less. In some embodiments, thehydrated polysialate of formula (G) comprises a poly(sialate) (z is 1 inempirical formula (G)), poly(sialate-siloxo) (z is 2 in empiricalformula (G)), or poly(sialate-disiloxo) (z is 3 empirical formula (G)).Before any curing, the poly(sialate), poly(sialate-siloxo), andpoly(sialate-disiloxo) each comprises a network of negatively chargedtetrahedral silicon tetroxides (formally SiO₄) and tetrahedral aluminumtetroxides (formally AlO₄) linked by shared oxygen atoms thereof,cations such that the overall charge of the aluminosilicates mineralpolymer is neutral, and water. The network of SiO₄ and AlO₄ tetrahedradefines structural cavities containing the cations M.

In some embodiments the invention modified geopolymer composition is ahighly organic polymer-adherent capable, modified geopolymercomposition, the highly organic polymer-adherent capable meaning thatthe highly organic polymer-adherent capable, modified geopolymercomposition, after being cured and dried in contact with a coating-readysurface of an organic polymer substrate, would produce a highly organicpolymer-adherent cured and dried modified geopolymer layer on thecoating-ready surface of the organic polymer substrate, the highlyorganic polymer-adherent cured and dried modified geopolymer layer beingcharacterizable as adhering to the coating-ready surface, or portionthereof, of the organic polymer substrate with a bond strength of 50.0kilopascals (kPa) or greater, wherein the highly organicpolymer-adherent capable, modified geopolymer composition is a waterconcentration- and Si/Al molar ratio-modified geopolymer composition,the water concentration- and Si/Al molar ratio-modified geopolymercomposition having less than 36.0 weight percent of water based on totalweight of the water concentration- and Si/Al molar ratio-modifiedgeopolymer; and the water concentration- and Si/Al molar ratio-modifiedgeopolymer composition comprising a hydrated polysialate of empiricalformula (G): (M)_(y)[-(—SiO₂)_(z)—AlO₂)]_(x).w H₂O (G), wherein each Mindependently is a cation of Group 1 of the Periodic Table of theElements; x is an integer of 2 or higher and represents a number ofpolysialate repeat units; y is an integer selected so that a ratio of yto x is greater than zero (y/x>0); z being the silicon/aluminum molarratio and is a rational or irrational number; and w is a rational orirrational number such that ratio of w to x represents a ratio of molesof water per polysialate repeat unit, wherein either (a) z is from 1.70to 3 or (b) z is from 1.9 to 3. Still more preferably z is from 1.70 to3. Even more preferably z is from 1.9 to 3, and yet more preferably z isfrom 1.9 to 3 and the water concentration- and Si/Al molarratio-modified geopolymer composition having less than 34.0 weightpercent of water based on total weight of the water concentration- andSi/Al molar ratio-modified geopolymer.

Examples of hydrated polysialates include, but are not limited to, thehydrated poly(sialate), hydrated poly(sialate-siloxo), and hydratedpoly(sialate-disiloxo) that have the following respective empiricalformulas (M-PS), (M-PSS), and (M-PSDS):

Poly(sialate): (M)_(y)-(—Si—O—Al—O—)_(x).w H₂O (M-PS), wherein molarratio of Si to Al is 1:1 (z=1);

Poly(sialate-siloxo): (M)_(y)-(Si—O—Al—O—Si—O—)_(x).w H₂O (M-PSS),wherein molar ratio of Si to Al is 2:1 (z=2); and

Poly(sialate-disiloxo): (M)_(y)-(Si—O—Al—O—Si—O—Si—O—)_(x).w H₂O(M-PSS), wherein molar ratio of Si to Al is 3:1 (z=3);

wherein x, y, w, and M independently are as defined for empiricalformula (G).

In some embodiments, the first mixture of the stabilizedgeopolymer-organic polymer latex composition or the highly organicpolymer-adherent capable, modified geopolymer composition, both beingmodified geopolymer compositions of the first embodiment, comprises afirst composite comprising, or formed by combining, two or more hydratedpolysialates, each hydrated polysialate of the composite independentlybeing of empirical formula (G) as described herein, the two or morehydrated polysialates, taken together, being characterizable with theempirical formula (G) and independently having an average value for eachof the x, y, and z, the average values independently being rational orirrational numbers. In some embodiments, the modified geopolymercomposition of the first embodiment comprises a second compositecomprising, or formed by combining, the modified geopolymer compositionof (i) and the modified geopolymer composition of (ii), both of thefirst embodiment. In some embodiments, the first or second composite, orboth, do not contain a calcium based oxide.

Unmodified geopolymer compositions useful for preparing the modifiedgeopolymer compositions of the present invention typically can beprepared by chemical dissolution and subsequent recondensation ofvarious aluminosilicates oxides and silicates in the presence ofhydroxide anions (O(H)⁻). In some embodiments, prepare an aqueous sodiumsilicate mixture (e.g., a sodium silicate solution) by combining water,sodium hydroxide, and a fumed silica. Combine the aqueous sodiumsilicate mixture with a source of aluminum oxides (e.g., a calcinedkaolin clay) to give an unmodified geopolymer composition. For example,prepare a predetermined sodium silicate solution by combiningpredetermined amounts of water, sodium hydroxide and fumed silica togive the predetermined sodium silicate solution formally containing 72weight percent (wt %) water, 10 wt % sodium hydroxide, and 18 wt % fumedsilica. Combine the predetermined sodium silicate solution with apredetermined amount of calcined kaolin clay to give an unmodifiedgeopolymer composition formally containing 29 wt % calcined kaolin clayand 71 wt % of the sodium silicate solution. Preferably, the modifiedgeopolymer compositions of the present invention comprise, or areprepared from, the aqueous sodium silicate mixture.

Organic polymers useful as the organic polymer latexes, organic polymersubstrates, or both can be natural or synthetic organic polymers. Theterm “organic polymer” means a macromolecule comprising carbon andhydrogen, the macromolecule comprising a plurality of repeat units, eachrepeat unit comprising a residual formed from a monomer, each monomerbeing the same as or different than another monomer. Where the monomersthat formed the residuals of the macromolecule are all the same, theresiduals can be the same or different from each other (e.g., terminalresiduals being different from interior residuals; post-polymerizationmodified residuals being different from unmodified residuals; or both).Examples of suitable monomers are hydrocarbon monomers (i.e., monomersthat consist of carbon and hydrogen) and heteroatom-containing monomers(i.e., monomers comprising carbon, hydrogen, and at least oneheteroatom, each heteroatom preferably being an oxygen, nitrogen,fluoro, chloro). Examples of suitable hydrocarbon monomers are ethylene,propylene, a (C₄-C₈)alpha-olefin, 1,4-butadiene, and styrene. Examplesof suitable heteroatom-containing monomers are a mixture of adipic acidand ethylenediamine, terephthalic acid and 1,4-butanediol,4-hydroxybenzoic acid, acrylic acid, and lactic acid. Monomers that aredicarboxylic acid derivatives such as, for example, dimethyldicarboxylic esters, dicarboxylic anhydrides (including cyclic and mixedcarboxylic acid anhydrides), and dicarboxylic acid dichlorides (i.e.,dicarboxoyl dichlorides) can be substituted for dicarboxylic acidmonomers.

Examples of organic polymers useful in the present invention thus arenatural rubber, polyethylene, polypropylene, a (C₄-C₈)alpha-olefin,poly(butadiene), and copolymerized mixtures thereof; polystyrenes;polycarbonates; polyesters, including polyethylene terephthalate,polylactic acid, and polybutylene terephthalate; polyacrylates;polymethacrylates; and interpolymers (e.g., copolymers) of any two ormore of the monomers employed in the manufacture of the foregoingorganic polymers. Unless otherwise noted, as used herein the term“butadiene” means 1,3-butadiene.

Preferably, the organic polymer substrate useful in the presentinvention comprises one or more of the example organic polymersmentioned in the immediately preceding paragraph. The aforementionedexample organic polymers are also useful in latex forms as the organicpolymer latexes, although the organic polymer latexes are not limitedthereto.

Organic polymer latexes comprise natural organic polymer latexes (e.g.,produced from hevea brasilienesis rubber tree) or, preferably, syntheticorganic polymer latexes. In some embodiments, the organic polymerlatexes useful in the present invention are water-borne organic polymerlatexes. The term “water-borne organic polymer latex” means a dispersionof microparticles of the organic polymer described previously in aliquid substance, the liquid substance having a molecular formula ofH₂O. Preferred water-borne organic polymer latexes are aqueousdispersions of microparticles of polypropylene, polybutylene,polystyrene, or poly(styrene-butadiene). In some embodiments, theorganic polymer latexes useful in the present invention are latexpowders. Preferably, the latex powders are redispersible in water.Preferred latex powders are homopolymer prepared from, and comprisingresidues of, vinyl acetate monomer or acrylic acid monomer or acopolymer that is a poly(vinyl acetate/vinyl versatate) copolymer, apoly(vinyl acetate/ethylene) copolymer, or a poly(styrene butadiene)copolymer. At least some latex powders are commercially available from,for example, Dow Wolff Cellulosics, a business unit of The Dow ChemicalCompany, Midland, Mich., USA. In some embodiments, the organic polymerlatexes useful in the present invention are a combination comprising awater-borne organic polymer latex and an organic polymer latex powder.

Preferably, the organic polymer latex, whether water-borne or in powderform, is characterized by a glass transition temperature of less than150 degrees Celsius (° C.). More preferably, the organic polymer latexis characterized by a glass transition temperature of less than 100° C.,still more preferably less than 75° C., even more preferably less than40° C.; and yet more preferably less than 30° C. Independently, theglass transition temperature is at least −40° C., preferably at least−20, more preferably at least −10° C., and even more preferably at least−5° C. In some embodiments, the invention modified geopolymercomposition is a stabilized geopolymer-organic polymer latexcomposition, the stabilized geopolymer-organic polymer latex compositioncomprising, or is formed by combining, a first mixture of a hydratedpolysialate and from 1.0 weight percent to 50 weight percent of anorganic polymer latex, weight percent of the organic polymer latex beingbased on total weight of the first mixture and the organic polymer latexbeing characterized by a glass transition temperature of less than 150°C.

Preferably, the organic polymer latex is present in the first mixturecomprising the stabilized geopolymer-organic polymer latex compositionof the first embodiment in a concentration of 40 wt % or less, morepreferably 35 wt % or less, and still more preferably 30 wt % or less,all based on total weight of the first mixture. While it is usuallydesirable to employ a minimum amount of the organic polymer latex thatwould be effective for providing a desired bonding strength for theadhering operative contact under the circumstances, in some embodiments,the concentration of the organic polymer latex in the first mixturecomprising the stabilized geopolymer-organic polymer latex compositionof the first embodiment preferably is at least 1 wt %, more preferablyat least 2 wt %, still more preferably at least 4 wt %, and even morepreferably at least 5 wt %, all based on total weight of the firstmixture. An example of a preferred concentration range is from about 5wt % to about 30 wt %, and more preferably from about 5 wt % to about 25wt %, based on total weight of the first mixture. Concentrations oforganic polymer latex that are provided later in the Examples areparticularly useful.

The term “latex stabilizer” means a substance that inhibits coagulationor agglomeration of organic polymer particles that comprise thewater-borne organic polymer latex. Latex stabilizers are known such as,for example, in U.S. Pat. No. 4,110,293. Examples of suitable latexstabilizers are proteins (e.g., gelatin and caseinate salts),carbohydrates (e.g., pectinates), glycols, and surfactants. Examples ofsuitable surfactants are anionic (i.e., sulfate, sulfonate, orcarboxylate containing) surfactants such as perfluorooctanesulfonate;cationic (i.e., quaternary ammonium containing) surfactants such ascetyl trimethylammonium bromide; zwitterionic (i.e., amphoteric)surfactants such as coco ampho glycinate; and nonionic surfactants suchas alkyl poly(ethylene oxide) and cetyl alcohol. Nonionic surfactantsare preferred. Commercially available latexes typically contain latexstabilizers in amounts suitable for the present invention. In someembodiments, additional amounts of latex stabilizers or additional latexstabilizers can be added when preparing the stabilizedgeopolymer-organic polymer latex composition.

Preferably, the latex stabilizer functions in the embodiments of theinvention stabilized geopolymer-organic polymer latex composition inwhich it is used as a means of stabilizing the water-borne organicpolymer latex of the first mixture against coagulation or agglomerationfor a time until the invention stabilized geopolymer-organic polymerlatex composition is ready for being cured or cured and dried (e.g.,hardening and having water removed therefrom). The latex stabilizer ispresent in the second mixture in a coagulating inhibiting amount, whichis sufficient to inhibit coagulation of the water-borne organic polymerlatex by 50% or more, preferably 75% or more, and more preferably 90% ormore within 1 hour, preferably until completion of the contacting step,more preferably until start of the drying step, and still morepreferably until start of the curing step of the second embodiment.Preferably, the coagulating inhibiting amount means the latex stabilizeris present in the second mixture comprising the water-borne organicpolymer latex and latex stabilizer, the latex stabilizer being presentin at least 1.0 wt %, more preferably at least 2.0 wt %, still morepreferably at least 3.0 wt %, and even more preferably at least 4.0 wt%; and preferably 9.0 wt % or less, more preferably 8.0 wt % or less,still more preferably 7.0 wt % or less, and even more preferably 6.0 wt% or less, based on total weight of the second mixture.

The organic polymer substrates can be employed in the present inventionin any form or shape. Examples of suitable forms of the organic polymersubstrates are solids and foams. Examples of suitable shapes are films,sheets, fibers, particles, and woven or non-woven fabrics ofthermoplastics. The organic polymer substrates can be prepared by anyconventional method such as casting, molding, and extrusion. The term“organic polymer substrate” means a base material comprising the organicpolymer described previously to which another material is contacted,adhered to, or both. A preferred organic polymer substrate is apolystyrene. The term “film” with respect to describing a substrate formof the organic polymer means a material of any desired length or widthand having a thickness from 0.001 centimeter (cm) to 0.1 cm. The term“sheet” means a material of any desired length or width and having athickness from 0.1 cm to 10 cm. Preferably, the substrate ischaracterized by surface porosity (e.g., as for foams). In someembodiments, the organic polymer substrate comprises a laminate of theorganic polymer substrate and one or more layers of the same ordifferent organic polymer substrate or any other suitable material suchas, for example, wood, paper, metal, cloth, or oxides of one or moremetal or metalloids, exemplified by clay, talc, silica, alumina, siliconnitride, or stone, as one or more layers of a multilayer structure or asa component of one or more layers provided that the organic polymersubstrate has an exposed surface capable of being coated with theinvention modified geopolymer composition.

Preferably, the geopolymer-coated organic polymer substrate comprises ageopolymer-coated article. That is, in some embodiments the invention isan article comprising the geopolymer-coated organic polymer substrate.In some embodiments the article comprises a geopolymer-coated automotivecomponent, building component, outdoor article, or geopolymer-linedinfrastructure component. More preferably the organic polymer substrateof the geopolymer-coated organic polymer substrate comprisespolystyrene. Examples of such geopolymer-coated articles have beendescribed previously herein. The geopolymer-coated articles can becoated in part or in whole. For example, the geopolymer-coated articlescan be coated on interior surfaces, exterior surfaces, or a combinationthereof. Preferably, the cured and dried modified geopolymer layerscomprising the geopolymer-coated articles have not cracked, peeled, orbubbled.

The modified geopolymer compositions of the first embodiment can becontacted to the coating-ready surface, or the portion thereof, of theorganic polymer substrate using any contacting methods as would be knownin the art. Examples of suitable contacting methods are spreading (e.g.,by pumping, mechanically pushing, or flowing), spraying, casting,molding, forming, and stamping. The contacting step provides themodified geopolymer precursor layer in physical contact with thecoating-ready surface, or the portion thereof, of the organic polymersubstrate. Preferably, the modified geopolymer precursor layer ischaracterized by a thickness, more preferably a uniform thickness. Themodified geopolymer precursor layer is also characterized as having adrying-ready exposed surface from which at least 30 wt % of the water ofthe modified geopolymer precursor layer is removed in the drying step.Preferably, the drying-ready exposed surface of the modified geopolymerprecursor layer is temporarily covered with a water barrier material(e.g., a polymer membrane or glass) during the curing step, and thenuncovered before the drying step.

Drying (i.e., removing water from) the cured modified geopolymerprecursor layer preferably comprises evaporation, stripping,freeze-drying, or a combination thereof. Drying can be done at ambientpressure (e.g., 101 kPa), elevated pressure (e.g., greater than 110 kPa,but preferably less than 120 kPa), or reduced pressure (e.g., less than95 kPa). Drying can be done at any temperature suitable for removingsome water from the modified geopolymer composition. Preferably, thedrying temperature is 100 degrees Celsius (° C.) or less, morepreferably less than 75° C., still more preferably less than 50° C., andeven more preferably less than 40° C.; and independently preferably atleast −10° C., more preferably at least −5, still more preferably atleast 10° C., and even more preferably at least 15° C. In someembodiments, drying is done at ambient temperature (e.g., 10° C. to 40°C.) and comprises evaporation.

Preferably, removing water is characterizable as being at the dryingtemperature, the drying temperature preferably being greater than theglass transition temperature of the organic polymer latex in embodimentsemploying the organic polymer latex. The term “drying temperature” meansa degree of hotness or coldness at which at least 30 wt % of water isremoved from the cured modified geopolymer precursor layer. Preferablyat least 50 wt %, more preferably at least 60 wt %, still morepreferably at least 70 wt %, and even more preferably at least 75 wt %of water is removed from the cured modified geopolymer precursor layerduring the drying step of the method of the second embodiment to givethe dried and cured modified geopolymer layer. Where an organic polymerlatex exhibits multiple glass transition temperatures, at least one andpreferably the lowest one of the multiple glass transition temperaturesis less than the drying temperature of the cured modified geopolymerprecursor layer.

Curing the modified geopolymer precursor layer to give the curedmodified geopolymer precursor layer can be done at any temperaturesuitable for curing the modified geopolymer composition. The term“curing temperature” means a degree of hotness or coldness at which thestabilized geopolymer-organic polymer latex composition or waterconcentration- and Si/Al molar ratio-modified geopolymer composition ishardened by allowing bonding thereof. Preferably curing is done at acuring temperature that is ambient temperature and, more preferably, acuring temperature of from 20° C. to 40° C. Curing and dryingtemperatures and pressures may be the same or different.

As mentioned previously, curing and drying the modified geopolymerprecursor layer gives the cured and dried modified geopolymer layer inadhering operative contact with the coating-ready surface, or portionthereof, of the organic polymer substrate. The adhering operativecontact meaning adhering to the coating-ready surface, or portionthereof, of the organic polymer substrate with a bond strength of 30.0kilopascals (kPa) or greater, more preferably 49 kPa or greater, stillmore preferably 70 kPa or greater, and even more preferably 100 kPa orgreater; and in some embodiments preferably about 150 kPa or lower, allwhen tested by the tensile pull test method described in the immediatelyfollowing paragraph. Where the modified geopolymer precursor layercomprises the stabilized geopolymer-organic polymer latex composition ofthe first embodiment, preferably, the stabilized geopolymer-organicpolymer latex composition is characterizable as being highly organicpolymer-adherent capable. That is, the stabilized geopolymer-organicpolymer latex composition, after being cured and dried in contact with acoating-ready surface of an organic polymer substrate, would produce ahighly organic polymer-adherent cured and dried geopolymer-organicpolymer latex layer on the coating-ready surface of the organic polymersubstrate, the highly organic polymer-adherent cured and driedgeopolymer-organic polymer latex layer being characterizable as adheringto the coating-ready surface, or portion thereof, of the organic polymersubstrate with a bond strength of 50.0 kilopascals (kPa) or greater whentested by the tensile pull test method described in the immediatelyfollowing paragraph.

Tensile Pull Test Method:

Step (a): Preparation of Cured and Dried 3-Layer Test Sample.

Obtain two pieces of an organic polymer substrate (e.g., polystyrenefoam) sample, each sample piece having dimensions of 2 inches (5.1centimeters (cm) by 2 inches (5.1 cm) square by 1 inch (2.54 cm) height.Separately coat a first 4 square inch (26 square cm) face of each one ofthe sample pieces with a test geopolymer composition, and hand press theresulting geopolymer layers together to give a three-layer laminatecomposite precursor sample comprising a bottom organic polymer substratelayer, a middle geopolymer layer, and a top organic polymer substratelayer. Wipe off any excess test geopolymer composition from edges of theprecursor sample. Repeat four times to give a total of five precursorsamples. Separately wrap the precursor samples in a plastic wrap (e.g.,a polyvinylidene chloride wrap) or place the precursor samples in apartially filled water bath sealed with an air tight lid, and place theresulting plastic wrapped precursor samples or the precursor samplessealed in the partially filled water bath in a 45° C. oven for overnight(e.g., 12 hours to 24 hours) to cure the geopolymer (i.e., harden thegeopolymer). (Alternatively, cure and dry precursor samples at ambienttemperature (about 20° C.) in an open (i.e., uncovered) environment(i.e., without wrapping the precursor samples in the plastic wrap orplacing the precursor samples in a sealed water bath) for a minimum of 2days and, preferably for about 7 days, as may be desirable underparticular circumstances.) Remove the resulting cured precursor samplesfrom the oven, remove the plastic wrap or from the partially filledwater bath, and allow the unwrapped cured precursor samples to dry atroom temperature to a constant weight to give cured and dried 3-layertest samples.

Step (b): Preparation of 5-Layer Final Test Sample

For each of the cured and dried 3-layer test samples of step (a), applya 2-part epoxy (3M Scotch-Weld epoxy adhesive 2216 B/A) to an outside(bottom) face of its bottom organic polymer substrate layer and anoutside (top) face of its top organic polymer substrate layer. Contacteach epoxy-containing outside face of the cured and dried test sample toa different one of two 2 inch (2.54 cm) by 2 inch (2.54 cm) steelplates. Allow the epoxy to dry for at least 24 hours to give afive-layer final test sample having opposing bottom and top steel platelayers.

Step (c): Tensile Pull Strength Testing.

Measure tensile pull strength of the five-layer final test samples ofstep (b) with an Instron (model 4204 or 5585) instrument. Use testparameters described in ASTM D 1623, which are particularly useful fortensile pull testing of polystyrene foam at a cross head speed of 0.05inch per minute (0.13 cm per minute).

COMPARATIVE EXAMPLES (NON-INVENTION)

Comparative Examples are provided herein as a contrast to certainembodiments of the present invention and are not meant to be construedas being either prior art or representative of non-invention examples.

Comparative Examples A1a to A1d Preparing Unmodified GeopolymerCompositions (Lacking the Organic Polymer Latex and Latex Stabilizers)(Water Contents Based on Total Weight of Unmodified GeopolymerComposition)

A1a: Prepare a sodium silicate solution by combining ingredients 61.9 gwater, 19.65 g solid sodium hydroxide, and 18.45 g of fumed silica. To a10 g portion of the sodium silicate solution add 4 g of calcined kaolinclay, and mix the resulting mixture to give the geopolymer compositionof Comparative Example A1a. Water content=47.3 wt % and Si/Al molarratio of 1.85.

A1b: Repeat the general procedure of Comparative Example 1a except withthe following ingredients and amounts: 56.26 g water, 21.47 g NaOH,22.26 g fumed silica and 65.82 g calcined kaolin to give geopolymercomposition of Comparative Example A1b (molar ratios: Si/Al=1.625;Na/Al=0.899) and water content=36.8 wt %.

A1c: Repeat the general procedure of Comparative Example 1a except withthe following ingredients and amounts: 52.78 g water, 20.16 g NaOH,27.06 fumed silica, and 55.56 g calcined kaolin to give geopolymercomposition of Comparative Example A1e (molar ratios: Si/Al=1.9;Na/Al=1.0) and water content=36.8 wt %.

A1d: Repeat the general procedure of Comparative Example 1a except withthe following ingredients and amounts: 52.31 g water, 23.41 g NaOH,24.27 fumed silica, and 71.76 g calcined kaolin to give geopolymercomposition of Comparative Example A1d (molar ratios: Si/Al=1.625;Na/Al=0.899) and water content=33.5 wt %.

Comparative Examples B1a to B1d Five-layer Final Test Samples forTensile Pull Test Method

B1a to B1d: Respectively using the preparation of steps (a) and (b) ofthe previously described the tensile pull test method and the unmodifiedgeopolymer of one of Comparative Examples A1a to A1d instead of the testgeopolymer composition, with each unmodified geopolymer prepare 5five-layer final test samples of Comparative Examples B1a to B1d.Determine average adhesion strength of the five-layer final test samplesaccording to step (c) of the previously described tensile pull testmethod. The tensile pull test results are recorded later in Table 1.

EXAMPLES OF THE PRESENT INVENTION

Non-limiting examples of the present invention are described below. Insome embodiments, the present invention is as described in the examples.

Example A1 Stabilized Geopolymer-organic Polymer Latex CompositionContaining 6.5 Wt % Water-borne Poly(styrene-butadiene) Latex

Repeat the general procedure of Comparative Example A1a except with 52.0g water, 19.65 g NaOH, 18.45 g silica, and 40 g calcined kaolin to givean unmodified geopolymer composition. To the unmodified geopolymercomposition add a weighed amount (19.6 g) of Latex DL 460 (apolyglycol-36 (PG-36) stabilized water-borne poly(styrene-butadiene)latex commercially available from The Dow Chemical Company, Midland,Mich., USA, having a T_(g)=8° C.) to give a modified geopolymercomposition that is the stabilized geopolymer-organic polymer latexcomposition of Example A1 containing 6.5 wt % of water-bornepoly(styrene-butadiene) latex and 44.2 wt % water content, both based ontotal weight of the stabilized geopolymer-organic polymer latexcomposition, and a Si/Al molar ratio of 1.85.

Examples A2 to A4 Stabilized Geopolymer-organic Polymer LatexCompositions Respectively Containing 16.7 Wt %, 20 Wt %, and 23.1 Wt %Water-borne Poly(styrene-butadiene) Latex a Water Content of 39.5 Wt %,37.9 Wt %, and 36.4 Wt %, Respectively, and each having a Si/Al MolarRatio of 1.85

Repeat the general procedure of Comparative Example A1a three timeswith: (i) 33.9 g water, 19.65 g NaOH, 18.45 g silica, 40 g calcinedkaolin, (ii) 26.9 g water, 19.65 g NaOH, 18.45 g silica, 40 g calcinedkaolin, or (iii) 19.9 g water, 19.65 g NaOH, 18.45 g silica, 40 gcalcined kaolin to give respective unmodified geopolymer compositions.Repeat the general procedure of Example A1 with the respectiveunmodified geopolymer compositions and higher weighed amounts (56.0 g,70.0 g, and 84.0 g, respectively) of Latex DL 460 (described above) togive instead the stabilized geopolymer-organic polymer latex compositionof Examples A2 to A4 respectively containing 16.7 wt %, 20 wt %, and23.1 wt % of water-borne poly(styrene-butadiene) latex and a watercontent of 39.5 wt %, 37.9 wt %, and 36.4 wt %, respectively, all basedon total weight of the stabilized geopolymer-organic polymer latexcompositions, and each having a Si/Al molar ratio of 1.85.

Examples A5a to A5c Stabilized Geopolymer-organic Polymer LatexCompositions Respectively Containing 4.8 Wt %, 9.1 Wt %, and 17 Wt %Poly(vinyl acetate/ethylene) Latex Powder; having Water Content=36.8 Wt%; and Si/Al Molar Ratio=1.625. Preparation Described Later Examples A6ato A6d Stabilized Geopolymer-organic Polymer Latex CompositionsRespectively Containing 4.8 Wt %, 9.1 Wt %, 23 Wt %, and 33 Wt %Poly(styrene-butadiene) Latex Powder; having Water Content=36.8 Wt %;and Si/Al Molar Ratio=1.625. Preparation Described Later Examples A7a toA7d Stabilized Geopolymer-organic Polymer Latex CompositionsRespectively Containing 4.8 Wt %, 9.1 Wt %, 17 Wt %, and 23 wt %Polyacrylic Acid Latex Powder; having Water Content=36.8 Wt %; and Si/AlMolar Ratio=1.625. Preparation Described Later Preparation of theStabilized Geopolymer-Organic Polymer Latex Composition of Examples A5ato A7d

Separately repeat the general procedure of Example A1 except (i) insteadof the unmodified geopolymer composition of Comparative Example A1a usethe unmodified geopolymer composition of Comparative Example A1b; and(ii) instead of Latex DL 460 use appropriate weighed amounts of eitherpoly(vinyl acetate/ethylene) latex powder having a T_(g)=3° C. (ExamplesA5a to A5c); or poly(styrene-butadiene) latex powder having a T_(g)=8°C. (Examples A6a to A6d); or polyacrylic acid latex powder having aT_(g)=10° C. (Examples A7a to A7d). These preparations give modifiedgeopolymer compositions that are the stabilized geopolymer-organicpolymer latex compositions respectively containing 4.8 wt %, 9.1 wt %,and 17 wt % poly(vinyl acetate/ethylene) latex powder of Examples A5a toA5c; stabilized geopolymer-organic polymer latex compositionsrespectively containing 4.8 wt %, 9.1 wt %, 23 wt %, and 33 wt %poly(styrene-butadiene) latex powder of Examples A6a to A6d; andstabilized geopolymer-organic polymer latex compositions respectivelycontaining 4.8 wt %, 9.1 wt %, 17 wt %, and 23 wt % polyacrylic acidlatex powder of Examples A7a to A7d, and all of the stabilizedgeopolymer-organic polymer latex composition of Examples A5a to A7dhaving water content=36.8 wt %; and Si/Al molar ratio=1.625.

Example A8 Water Concentration- and Si/Al Molar Ratio-modifiedGeopolymer Composition having Water Content=33.5 Wt % and a Si/Al MolarRatio of 1.9

Prepare a water concentration- and Si/Al molar ratio-modified geopolymercomposition having a reduced water content compared to water content ofthe unmodified geopolymer composition of Comparative Example A1c byemploying a reduced water content sodium silicate solution having 48.8 gwater, 21.9 g NaOH, 29.3 g silica, and combining the reduced watercontent sodium silicate solution with 60.2 g calcined kaolin to give ahighly organic polymer-adherent capable, modified geopolymer compositionthat is the water concentration- and Si/Al molar ratio-modifiedgeopolymer composition of Example A8 having a water content=33.5 wt %and a Si/Al molar ratio of 1.9.

Examples B1 to B4 Five-layer Final Test Samples Comprising a StabilizedGeopolymer-organic Polymer Latex Composition of any One of Examples A1to A4, Respectively. Preparation and Testing Described Later ExamplesB5a to B5c; B6a to B6d; and B7a to B7d Five-layer Final Test SamplesComprising a Stabilized Geopolymer-organic Polymer Latex Composition ofany One of Examples A5a to A5c; A6a to A6d; and A7a to A7d,Respectively. Preparation and Testing Described Later Example B8Five-layer Final Test Samples Comprising the StabilizedGeopolymer-organic Polymer Latex Composition of Example A8. Preparationand Testing Described Later Preparation of the Five-Layer Final TestSamples of Examples B1 to B8

Repeat the procedure of steps (a) and (b) of the tensile pull testmethod four times for each of the stabilized geopolymer-organic polymerlatex composition of Examples A1 to A4, B5a to B5c; B6a to B6d; and B7ato B7d, or B8, respectively, instead of the test geopolymer compositionto give four five-layer final test samples for each of Examples B1 toB8. Determine average adhesion strengths according to the previouslydescribed step (c) of the tensile pull test method with each of the fourfive-layer final test samples. The type of modification of the modifiedgeopolymer compositions, weight percents, and tensile pull test resultsare recorded below in Table 1.

TABLE 1 tensile pull test results Tensile Modification of geopolymerWeight Pull 95% Sample (water content (wt %) and Si/Al molar ratioPercent of Strength Confidence Number (Si/Al)) latex (wt %) (kPa) (kPa)CE* B1a None 0 10  N/a** (water content = 47.3 wt %; Si/Al = 1.85) CEB1b None 0 14 N/a (water content = 36.8 wt %; Si/Al = 1.6) CE B1c None 019 N/a (water content = 36.8 wt %; Si/Al = 1.9) CE B1d None 0 8 N/a(water content = 33.5 wt %; Si/Al = 1.6) B1 water-bornepoly(styrene-butadiene) latex 6.5 26   ±2.9 (water content = 44.2 wt %;Si/Al = 1.85) B2 water-borne poly(styrene-butadiene) latex 16.7 25  ±2.8 (water content = 39.5 wt %; Si/Al = 1.85) B3 water-bornepoly(styrene-butadiene) latex 20.0 32 N/a (water content = 37.9 wt %;Si/Al = 1.85) B4 water-borne poly(styrene-butadiene) latex 23.15 26  ±2.8 (water content = 36.4 wt %; Si/Al = 1.85) B5a poly(vinylacetate/ethylene) latex powder 4.8 9 N/a (water content = 36.8 wt %;Si/Al = 1.625) B5b poly(vinyl acetate/ethylene) latex powder 9.1 18 N/a(water content = 36.8 wt %; Si/Al = 1.625) B5c poly(vinylacetate/ethylene) latex powder 17 8 N/a (water content = 36.8 wt %;Si/Al = 1.625) B6a poly(styrene-butadiene) latex powder 4.8 140 N/a(water content = 36.8 wt %; Si/Al = 1.625) B6b poly(styrene-butadiene)latex powder 9.1 68 ±21 (water content = 36.8 wt %; Si/Al = 1.625) B6cpoly(styrene-butadiene) latex powder 23 58 ±14 (water content = 36.8 wt%; Si/Al = 1.625) B6d poly(styrene-butadiene) latex powder 33 49 ±11(water content = 36.8 wt %; Si/Al = 1.625) B7a polyacrylic acid latexpowder 4.8 43 N/a (water content = 36.8 wt %; Si/Al = 1.625) B7bpolyacrylic acid latex powder 9.1 63 ±24 (water content = 36.8 wt %;Si/Al = 1.625) B7c polyacrylic acid latex powder 17 85.5 ±24 (watercontent = 36.8 wt %; Si/Al = 1.625) B7d polyacrylic acid latex powder 2373.8 ±30 (water content = 36.8 wt %; Si/Al = 1.625) B8 (reduced) waterconcentration- and Si/Al molar 0 77 N/a ratio-modified 92 (water content= 33.5 wt %, Si/Al = 1.9) *CE means Comparative Example; **N/a means notavailable.

As shown by the Examples, the invention stabilized geopolymer-organicpolymer latex composition is capable of coating a coating-ready surfaceof an organic polymer substrate and, after curing and drying, forms anadherent, and in some cases a highly adherent, coating layer on thecoating ready surface of the organic polymer substrate. In contrast, thecompositions consisting of unmodified geopolymer, and thus lacking theorganic polymer latex or not having a combination of reduced watercontent and increased Si/Al molar ratio, do not adhere, or adhere weaklyto coating-ready surfaces of organic polymer substrates.

While the present invention has been described above according to itspreferred embodiments, it can be modified within the spirit and scope ofthis disclosure. This application is therefore intended to cover anyvariations, uses, or adaptations of the present invention using thegeneral principles disclosed herein. Further, the application isintended to cover such departures from the present disclosure as comewithin the known or customary practice in the art to which this presentinvention pertains and which fall within the limits of the followingclaims.

What is claimed is:
 1. A modified geopolymer composition that comprises(i) a stabilized geopolymer-organic polymer latex composition comprisinga mixture of a geopolymer and an organic polymer latex, wherein thegeopolymer is an inorganic aluminosilicate composition having less than36.0 weight percent of water, based on the total weight of water andgeopolymer, and having a Si/Al molar ratio of from 1.70 to 3.0.
 2. Amodified geopolymer composition that is a stabilized geopolymer-organicpolymer latex composition comprising a uniform mixture of a geopolymerand an organic polymer latex.
 3. The modified geopolymer composition asin claim 2, the stabilized geopolymer-organic polymer latex compositioncomprising a first mixture of a hydrated polysialate and from 1.0 weightpercent to 50 weight percent of an organic polymer latex, weight percentof the organic polymer latex being based on total weight of the firstmixture.
 4. The modified geopolymer composition as in claim 3, thehydrated polysialate being of empirical formula (G):(M)_(y)[-(—SiO₂)_(z)—AlO₂)]_(x).w H₂O (G), wherein each M independentlyis a cation of Group 1 of the Periodic Table of the Elements; x is aninteger of 2 or higher and represents a number of polysialate repeatunits; y is an integer selected so that a ratio of y to x is greaterthan zero (y/x >0); z is a rational or irrational number of from 1 to35; and w is a rational or irrational number such that ratio of w to xrepresents a ratio of moles of water per polysialate repeat unit.
 5. Themodified geopolymer composition as in claim 3, wherein the organicpolymer latex, which is used to form the first mixture, comprises asecond mixture comprising a water-borne organic polymer latex and from0.05 weight percent to 10 weight percent of a latex stabilizer, weightpercent of the latex stabilizer being based on total weight of thesecond mixture.
 6. The modified geopolymer composition as in claim 5,the water-borne organic polymer latex comprising a water-bornedispersion of polypropylene, polybutylene, polystyrene, orpoly(styrene-butadiene).
 7. The modified geopolymer composition as inclaim 3, wherein the organic polymer latex, which is used to form thefirst mixture, comprises an organic polymer latex powder.
 8. Themodified geopolymer composition as in claim 7, the organic polymer latexpowder comprising a homopolymer prepared from, and comprising residuesof, acrylic acid monomer or a poly(styrene butadiene) copolymer.
 9. Themodified geopolymer composition as in claim 2, the stabilizedgeopolymer-organic polymer latex composition, after being cured anddried in contact with a coating-ready surface of an organic polymersubstrate, has a bond strength of 50.0 kilopascals (kPa) or greater.